Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1310-2014 — TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient results from a connected instrument and sends them to a Laboratory Information System (LIS).

U.S. FDA — Device Enforcement · France · 2014-02-17 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1310-2014
Date of alert: 2014-02-17
Country / jurisdiction: France
Risk level: Class III
Risk type: recall
Brand: Technidata S.A.
Product category: device
Product type: Devices

Reported risk: If a conflict occurs between a Demography Query and a Result Transmission by the instrument, the TDWorkstation could send an incorrect patient demography to an instrument.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-1310-2014 — TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient results from a connected instrument and sends them to a Laboratory Information System (LIS).

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